Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:23453156-23453393 | Rare:81 | ||||
chr18:23503300-23503652 | Common:4; Rare:151 | ||||
chr18:23586360-23586532 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):3 | ||||
chr18:23872683-23873035 | Rare:86 | ||||
chr18:23884425-23884760 | Common:1; Rare:59 | ||||
chr18:24271603-24271757 | Common:2; Rare:44 | ||||
chr18:24397758-24398111 | Common:2; Rare:123 | ||||
chr18:24426620-24426786 | Common:3; Rare:65 | ||||
chr18:25351027-25351125 | Rare:35 | ||||
chr18:25352012-25352415 | Common:2; Rare:156 | ||||
chr18:26226140-26226478 | Common:3; Rare:106 | ||||
chr18:26546904-26547125 | Rare:75 | ||||
chr18:26549765-26549967 | Common:2; Rare:60 | ||||
chr18:26657380-26657481 | Rare:25 | ||||
chr18:31101248-31101590 | Common:10; Rare:92 |